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Study identifier: NCT07067580 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

Effect of Breathing Exercise on Pain and Quality of Recovery in After Transplantation Patients: A Randomized Controlled Trial

Condition: Transplantation · Pain Management · Quality of Recovery 40  ·  Sponsor: Ankara Yildirim Beyazıt University

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNoCheck eligibility criteria ↓
WhereAnkara, Turkey (Türkiye)

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The researchers will fill out the "Patient Introduction Form" for the patients who agreed to participate in the study after obtaining permission from the experimental group with the "Informed Consent Form" the day before the surgery. The breathing exercises will be taught and monitored by the researchers, and the researcher who will implement them is a nurse in the general surgery department. The experimental group will be trained on breathing exercises by the researcher the day before the surgery. The patients will be provided with 1 set (4 breaths) per hour of breathing exercises after the surgery. The patient's vital signs will be monitored before and after the breathing exercise. Patients will not have difficulty during the breathing exercise, and they will be provided with gradual interventions. Pain status will be monitored at 0, 2, 6, 12 and 24 hours during the 24-hour hospital stay. The recovery quality scale will be applied on the 1st and 3rd day after surgery. In the control group, after obtaining permission with the "Informed Consent Form" the day before the surgery, the patients who agreed to participate in the study will fill out the "Patient Introduction Form" by the researchers, and their pain status will be monitored at 0, 2, 6, 12 and 24 hours during the 24-hour hospital stay after the surgery. The recovery quality scale will be applied on the 1st and 3rd day after surgery. No intervention will be made to the patients in the control group, and they will be pr…

This description comes directly from the study's public registry record.

Talk to the study team

Tuba Yilmazer, PhD  ·  5079552804  ·  tyilmazer@aybu.edu.tr

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patients aged 18 and over, 65 and under, * Those who have had a transplant for the first time, * Patients who volunteer to participate in the study will be included in the study. Exclusion Criteria: * Hemodynamically unstable, * Those who may experience physical strain during breathing exercises and have a disease that may cause increased intra-abdominal pressure (e.g. bleeding hemorrhoids, hernias of all kinds, persistent cough, severe back pain, heart diseases, high blood pressure, urinary incontinence, epilepsy), * Those with early complications * Those with neurological or psychological problems, * Those who were transferred to the intensive care unit after surgery, * Emergency and unplanned cases will be excluded from the scope of the research.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Ankara Yıldırım Beyazıt UniversityAnkara, Turkey (Türkiye)Recruiting

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Ankara

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